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rs11547346

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs11547346(A;C)
Make rs11547346(C;C)
ReferenceGRCh38 38.1/141
Chromosome6
Position31271569
GeneHLA-C
is asnp
is mentioned by
dbSNPrs11547346
ebirs11547346
HLIrs11547346
Exacrs11547346
Varsomers11547346
Maprs11547346
PheGenIrs11547346
hapmaprs11547346
1000 genomesrs11547346
hgdprs11547346
ensemblrs11547346
gopubmedrs11547346
geneviewrs11547346
scholarrs11547346
googlers11547346
pharmgkbrs11547346
gwascentralrs11547346
openSNPrs11547346
23andMers11547346
23andMe allrs11547346
SNP Nexus

SNPshotrs11547346
SNPdbers11547346
MSV3drs11547346
GWAS Ctlgrs11547346
GMAF0.03352
Max Magnitude0
ClinVar
Risk rs11547346(C;C)
Alt rs11547346(C;C)
Reference rs11547346(A;A)
Significance Histocompatibility
Disease
Variation info
Gene HLA-C
CLNDBN
Reversed 1
HGVS NC_000006.11:g.31239346T>G
CLNSRC
CLNACC